rs8105815
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8105815(G;G) |
| Make rs8105815(G;T) |
| Make rs8105815(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 41167943 |
| Gene | CYP2A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8105815 |
| dbSNP (classic) | rs8105815 |
| ClinGen | rs8105815 |
| ebi | rs8105815 |
| HLI | rs8105815 |
| Exac | rs8105815 |
| Gnomad | rs8105815 |
| Varsome | rs8105815 |
| LitVar | rs8105815 |
| Map | rs8105815 |
| PheGenI | rs8105815 |
| Biobank | rs8105815 |
| 1000 genomes | rs8105815 |
| hgdp | rs8105815 |
| ensembl | rs8105815 |
| geneview | rs8105815 |
| scholar | rs8105815 |
| rs8105815 | |
| pharmgkb | rs8105815 |
| gwascentral | rs8105815 |
| openSNP | rs8105815 |
| 23andMe | rs8105815 |
| SNPshot | rs8105815 |
| SNPdbe | rs8105815 |
| MSV3d | rs8105815 |
| GWAS Ctlg | rs8105815 |
| GMAF | 0.1749 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22210626 ]
|
| Trait | |
| Title | Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. |
| Risk Allele | |
| P-val | 0.000008 |
| Odds Ratio | 1.3918 None |
